www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"69953-517-01" National Drug Code (NDC)

Morning After 1 BLISTER PACK in 1 CARTON (69953-517-01) / 1 mg in 1 BLISTER PACK
(Rapha Pharmaceuticals, Inc.)

NDC Code69953-517-01
Package Description1 BLISTER PACK in 1 CARTON (69953-517-01) / 1 mg in 1 BLISTER PACK
Product NDC69953-517
Product Type NameHUMAN OTC DRUG
Proprietary NameMorning After
Non-Proprietary NameLevonorgestrel
Dosage FormTABLET
UsageORAL
Start Marketing Date20221230
Marketing Category NameANDA
Application NumberANDA205329
ManufacturerRapha Pharmaceuticals, Inc.
Substance NameLEVONORGESTREL
Strength1.5
Strength Unitmg/1.5mg
Pharmacy ClassesInhibit Ovum Fertilization [PE], Progesterone Congeners [CS], Progesterone Congeners [CS], Progestin [EPC], Progestin-containing Intrauterine Device [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69953-517-01





Copyright © 2007-2024 www.ndcvalidator.com